FDA Inspection 1224183 — Eurofins Amatsi Analytics

Eurofins Amatsi Analytics — FEI 3006118993

The FDA completed an inspection of Eurofins Amatsi Analytics on Nov 3, 2023 in Fontenilles. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 3, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Fontenilles (France)

Additional details

Bioanalytical BA/BE

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.